Kawamura Rie 河村理恵

… Alternative Names

Researcher Number	20735534
Other IDs
Affiliation (Current)	2021: 藤田医科大学, 総合医科学研究所, 助教
Affiliation (based on the past Project Information) *help	2018 – 2019: 藤田医科大学, 総合医科学研究所, 助教 2015 – 2017: 信州大学, 医学部, 助教(特定雇用)
Review Section/Research Field	Principal Investigator Learning support system Except Principal Investigator Human genetics / Basic Section 56040:Obstetrics and gynecology-related
Keywords	Principal Investigator 遺伝学的検査 / 細胞遺伝 / cytogenetics / 遺伝医学 / 染色体検査 / 教材開発 / マイクロアレイ染色体検査 Except Principal Investigator １細胞解析 / 相同染色体 / RNA-FISH … More

体外受精した初期胚において染色体数的異常胚を誘発する要因の解明Ongoing
- Principal Investigator
  
  宮井俊輔
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  Fujita Health University
Development of a hands-on cytogenetics training program for genomic medical workersPrincipal Investigator
- Principal Investigator
  
  KAWAMURA Rie
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Learning support system
- Research Institution
  Fujita Health University
  Shinshu University
Research for single cell expression analysis and epigenetic mechanism using RNA-FISH analyses
- Principal Investigator
  
  Wakui Keiko
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Shinshu University

All 2020 2019 2018 2017 2016 2015

All Journal Article Presentation

[Journal Article] A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia2020
- Author(s)
  Kawamura R, Kato T, Miyai S, Suzuki F, Naru Y, Kato M, Tanaka K, Nagasaka M, Tsutsumi M, Inagaki H, Ioroi T, Yoshida M, Nao T, Conlin LK, Iijima K, Kurahashi H, Taniguchi-Ikeda M.
- Journal Title
  
  Journal of Human Genetics
  
  Volume: -
- DOI
  10.1038/s10038-020-0748-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-17K00481, KAKENHI-PROJECT-17K11259
[Journal Article] Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome2019
- Author(s)
  Toshimitsu M, Nagaoka S, Kobori S, Ogawa M, Suzuki F, Kato T, Miyai S, Kawamura R, Inagaki H, Kurahashi H, Murotsuki J.
- Journal Title
  
  Case Reports in Obstetrics and Gynecology
  
  Volume: - Pages: 1-5
- DOI
  10.1155/2019/6753184
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-17K11259
[Journal Article] CTCFdeletion syndrome: clinical features and epigenetic delineation2017
- Author(s)
  Hori I, Kawamura R, Nakabayashi K, Watanabe H, Higashimoto K, Tomikawa J, Ieda D, Ohashi K, Negishi Y, Hattori A, Sugio Y, Wakui K, Hata K, Soejima H, Kurosawa K, Saitoh S
- Journal Title
  
  J Med Genet.
  
  Volume: 54 Pages: 836-842
- DOI
  10.1136/jmedgenet-2017-104854
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K07248, KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-26293365, KAKENHI-PROJECT-15K08330
[Presentation] Genetic counseling for preimplantation genetic diagnosis2019
- Author(s)
  河村理恵，森山育実，加藤麻希，河合美紀，宮井俊輔，倉橋浩樹
- Organizer
  第43回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-19K09790
[Presentation] dic(Y;22)と45,Xの核型をもつターナー症候群の一例2019
- Author(s)
  河村理恵，稲垣秀人，山田緑，鈴木史彦，成悠希，倉橋浩樹
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] Parthenogenetic maternalとdouble paternal alleleを有するキメラ症例の解析2019
- Author(s)
  河村理恵，加藤武馬，宮井俊輔，鈴木史彦，成悠希，田中敬子，長坂美和子，池田真理子，倉橋浩樹
- Organizer
  第41回日本小児遺伝学会学術集会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] 着床前診断を希望して来談されたクライエントの想いと遺伝カウンセリング2019
- Author(s)
  河村理恵，森山育実，加藤麻希，河合美紀，宮井俊輔，倉橋浩樹
- Organizer
  第43回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] Report of a 46,XX/46,XY with parthenogenetic chimera2018
- Author(s)
  河村理恵，加藤武馬，宮井俊輔，鈴木史彦，成悠希，田中敬子，長坂美和子，池田真理子，倉橋浩樹
- Organizer
  日本人類遺伝学会第63回大会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] マイクロアレイ染色体検査にて派生染色体に端部欠失が検出されなかった不均衡型転座症例2017
- Author(s)
  河村理恵
- Organizer
  日本人類遺伝学会第62回大会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] CTCF遺伝子欠失を認めた2女児の臨床的および遺伝学的検討2016
- Author(s)
  堀いくみ, 河村理恵, 中林一彦, 家田大輔, 大橋圭, 根岸豊, 服部文子, 杉尾嘉嗣, 涌井敬子, 黒澤健司, 秦健一郎, 副島英伸, 齋藤伸治
- Organizer
  第39回日本小児遺伝学会学術集会
- Place of Presentation
  慶應義塾大学三田北館ホール
- Year and Date
  2016-12-09
- Data Source
  KAKENHI-PROJECT-15K08330
[Presentation] Xp21欠失女性症例における不活化X染色体解析　 ―構造異常X染色体を識別するRNA/DNA-FISH解析―2015
- Author(s)
  河村理恵，伊波若葉，福嶋義光，涌井敬子
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  京王プラザホテル（新宿・東京）
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-15K08330
[Presentation] Establishment of a single-cell RNA/DNA-FISH method for detecting inactivation patterns of structural X chromosome abnormalities2015
- Author(s)
  Rie KAWAMURA, Wakaba IHA, Yoshimitsu FUKUSHIMA, Keiko WAKUI
- Organizer
  第10回European Cytogenetics Conference
- Place of Presentation
  ストラスブール（フランス）
- Year and Date
  2015-07-04
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08330

1. Wakui Keiko (50324249)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
2. 福嶋義光 (70273084)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
3. KOSHO Tomoki (90276311)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. SAITOH Shinji (00281824)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 高野亨子 (70392420)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 宮井俊輔 (50563350)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
7. 加藤武馬 (20387690)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
8. 斉藤伸治

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
9. 冨川順子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
10. 副島英伸

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. 秦健一郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kawamura Rie 河村 理恵

KAWAMURA Rie 河村 理恵

Research Projects

Research Products

Co-Researchers

体外受精した初期胚において染色体数的異常胚を誘発する要因の解明Ongoing

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Development of a hands-on cytogenetics training program for genomic medical workersPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Research for single cell expression analysis and epigenetic mechanism using RNA-FISH analyses

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] CTCFdeletion syndrome: clinical features and epigenetic delineation2017

Author(s)

Journal Title

DOI

Data Source

[Presentation] Genetic counseling for preimplantation genetic diagnosis2019

Author(s)

Organizer

Data Source

[Presentation] dic(Y;22)と45,Xの核型をもつターナー症候群の一例2019

Author(s)

Organizer

Data Source

[Presentation] Parthenogenetic maternalとdouble paternal alleleを有するキメラ症例の解析2019

Author(s)

Organizer

Data Source

[Presentation] 着床前診断を希望して来談されたクライエントの想いと遺伝カウンセリング2019

Author(s)

Organizer

Data Source

[Presentation] Report of a 46,XX/46,XY with parthenogenetic chimera2018

Author(s)

Organizer

Data Source

[Presentation] マイクロアレイ染色体検査にて派生染色体に端部欠失が検出されなかった不均衡型転座症例2017

Author(s)

Organizer

Data Source

[Presentation] CTCF遺伝子欠失を認めた2女児の臨床的および遺伝学的検討2016

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] Xp21欠失女性症例における不活化X染色体解析 ―構造異常X染色体を識別するRNA/DNA-FISH解析―2015

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] Establishment of a single-cell RNA/DNA-FISH method for detecting inactivation patterns of structural X chromosome abnormalities2015

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

Kawamura Rie 河村理恵

KAWAMURA Rie 河村理恵

[Presentation] Xp21欠失女性症例における不活化X染色体解析　 ―構造異常X染色体を識別するRNA/DNA-FISH解析―2015